Summary
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1.
It has been shown that in the Grignard-Wurtz synthesis of alkenylsilanes from 1-bromo-2-butenes, the latter undergo the same type of allyl rearrangement as in the synthesis of hydrocarbons, i.e., in the condensation of R- MgX
are formed. When R-X is condensed with
is formed.
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2.
Silicon analogs of olefins have been synthesized: (1-methylallyl)silane, 2-butenylsilane, methyl(1-methylallyl)silane, trichloro(1-methylallyl)silane, triethyl(1-methylallyl)silane, and trimethyl-3-pentenylsilane.
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Yu. P. Egorov and P. A. Bazhulin, Proc. Acad. Sci. USSR, 88, No. 4, 647 (1953).
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A. V. Topchiev, N. S. Nametkin, and A. A. Shcherbakova, Proc. Acad. Sci. USSR, 86, No. 3, 889 (1952).
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Petrov, A.D., Ponomarenko, V.A. & Boikov, V.I. Synthesis and properties of (1-methylallyl)- and 2-butenyl-silanes. Russ Chem Bull 3, 429–434 (1954). https://doi.org/10.1007/BF01167821
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DOI: https://doi.org/10.1007/BF01167821